Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_assertion> ?p ?o ?g. }
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- NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_assertion type Assertion NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_head.
- NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_assertion wasGeneratedBy ECO_0000218 NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_provenance.
- NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_assertion wasDerivedFrom uniprot-2016 NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_provenance.
- NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_assertion SIO_000772 11549681 NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_provenance.
- NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_assertion evidence source_evidence_curated NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_provenance.
- NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_assertion description "[Autosomal recessive segregation of a truncating mutation of anti-Müllerian type II receptor in a family affected by the persistent Müllerian duct syndrome contrasts with its dominant negative activity in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_provenance.